Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7556604

CCCCCCCCCCCCCCCCCC[P+](C)(C)CCCCCCCCCCCCCCCCCC.[Cl-]

nearest known ligand 0.58

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Hydrochloric Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
DNM1 Q05193 4/20 0.58
TSHR P16473 2/20 0.53
THRB P10828 1/20 0.53
OPRM1 P35372 1/20 0.48
SPHK1 Q9NYA1 1/20 0.44
LMNA P02545 2/20 0.43
GGPS1 O95749 2/20 0.42
ADH1B P00325 1/20 0.41
ADH1C P00326 1/20 0.41
ADH1A P07327 1/20 0.41
ADH4 P08319 1/20 0.41
ADH7 P40394 1/20 0.41
ALDH1A1 P00352 2/20 0.40
HSD17B10 Q99714 1/20 0.40

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Hydrochloric Acid SCHEMBL5084820 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL5087250 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL5092767 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL5091937 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL5092135 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL23576227 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL5087047 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL5088313 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Hydrochloric Acid SCHEMBL5086847 1.00 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1
Iodide SCHEMBL5087923 0.93 DNM1 (0.58) DNM1TSHRTHRBOPRM1SPHK1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 20 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10836841-B2 Process for producing epoxidized polymers COOPER TIRE & RUBBER COMPANY (US) 2020-11-17 US disclosed
US-20190127495-A1 PROCESS FOR PRODUCING EPOXIDIZED POLYMERS GOODYEAR TIRE & RUBBER COMPANY, THE 2019-05-02 US disclosed
EP-3440116-A1 PROCESS FOR PRODUCING EPOXIDIZED POLYMERS Cooper Tire & Rubber Company (US) 2019-02-13 EP disclosed
WO-2017176686-A1 PROCESS FOR PRODUCING EPOXIDIZED POLYMERS COOPER TIRE & RUBBER COMPANY (US) 2017-10-12 WO disclosed
US-20140155526-A1 POLYIMIDE COMPOSITION VARNISH, FILM USING THE SAME, AND METHOD OF MANUFACTURING THE POLYIMIDE COMPOSITION VARNISH SAMSUNG DISPLAY CO., LTD. (KR) 2014-06-05 US disclosed
EP-0946600-B1 METHOD FOR THE EPOXIDATION OF UNSATURATED POLYMERS SARTOMER CO INC (US) 2002-08-14 EP disclosed
EP-0973759-B1 CYCLOALIPHATIC EPOXIDES AND THE METHOD FOR MAKING THE SAME SARTOMER CO INC (US) 2002-07-24 EP disclosed
US-6084111-A Method for making cycloaliphatic epoxides SARTOMER TECHNOLOGIES INC. (US) 2000-07-04 US disclosed
EP-0973759-A2 CYCLOALIPHATIC EPOXIDES AND THE METHOD FOR MAKING THE SAME SARTOMER COMPANY INC. (US) 2000-01-26 EP disclosed
EP-0946534-A2 UNSATURATED (METH)ACRYLATE ESTERS CONTAINING EPOXIDIZED CYCLIC GROUPS AND PROCESS FOR PREPARING SARTOMER COMPANY, INC. (US) 1999-10-06 EP disclosed
EP-0946535-A1 ALKOXYLATED GLYCIDYL (METH)ACRYLATES AND METHOD OF PREPARATION SARTOMER COMPANY, INC. (US) 1999-10-06 EP disclosed
EP-0946600-A1 METHOD FOR THE EPOXIDATION OF UNSATURATED POLYMERS SARTOMER COMPANY, INC. (US) 1999-10-06 EP disclosed
WO-1998045349-A2 CYCLOALIPHATIC EPOXIDES AND THE METHOD FOR MAKING THE SAME SARTOMER COMPANY, INC. (US) 1998-10-15 WO disclosed
US-5789512-A Method for the epoxidation of unsaturated polymers SARTOMER COMPANY (US) 1998-08-04 US disclosed
WO-1998028287-A1 ALKOXYLATED GLYCIDYL (METH)ACRYLATES AND METHOD OF PREPARATION SARTOMER COMPANY, INC. (US) 1998-07-02 WO disclosed
WO-1998028286-A2 UNSATURATED (METH)ACRYLATE ESTERS CONTAINING AT LEAST ONE EPOXIDIZED CYCLIC GROUP AND PROCESS FOR PREPARING THEM SARTOMER COMPANY, INC. (US) 1998-07-02 WO disclosed
WO-1998028338-A1 METHOD FOR THE EPOXIDATION OF UNSATURATED POLYMERS SARTOMER COMPANY, INC. (US) 1998-07-02 WO disclosed
US-5767150-A Cycloaliphatic epoxide compounds SARTOMER COMPANY (US) 1998-06-16 US disclosed
US-5763629-A Alkoxylated glycidyl (meth)acrylates and method of preparation SARTOMER COMPANY (US) 1998-06-09 US disclosed
US-5036154-A Preparation of glycidyl esters THE DOW CHEMICAL COMPANY (US) 1991-07-30 US disclosed